A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121145



Internal ID19250203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:25686249..25687233hg38UCSC Ensembl
Outerchr15:25931396..25932380hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38985
hg19985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1180n106
Supporting Variantsnssv3964837, nssv3966201
SamplesKWS2, KWS1
Known GenesATP10A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121145
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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